Canonical Allele Identifier: PA108727
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 625260
ClinVar RCV Id: RCV000767288
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Leu178Gln
CA70052370
NM_000551.4:c.533T>A